ALX4 Antibody (Center) Blocking peptide
€363.00
In stock
SKU
AC-BP10386c
Background:
This gene encodes a paired-like homeodomain transcriptionfactor expressed in the mesenchyme of developing bones, limbs,hair, teeth, and mammary tissue. Mutations in this gene causeparietal foramina 2 (PFM2); an autosomal dominant diseasecharacterized by deficient ossification of the parietal bones.Mutations in this gene also cause a form of frontonasal dysplasiawith alopecia and hypogonadism; suggesting a role for this gene incraniofacial development, mesenchymal-epithelial communication, andhair follicle development. Deletion of a segment of chromosome 11containing this gene, del(11)(p11p12), causes Potocki-Shaffersyndrome (PSS); a syndrome characterized by craniofacial anomalies,mental retardation, multiple exostoses, and genital abnormalitiesin males. In mouse, this gene has been shown to use dualtranslation initiation sites located 16 codons apart. [provided byRefSeq].
Other Names:
Homeobox protein aristaless-like 4, ALX4, KIAA1788
Gene Name: ALX4
Gene ID: 60529
Primary Accession: Q9H161
Other Accession: NP_068745.2
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
This gene encodes a paired-like homeodomain transcriptionfactor expressed in the mesenchyme of developing bones, limbs,hair, teeth, and mammary tissue. Mutations in this gene causeparietal foramina 2 (PFM2); an autosomal dominant diseasecharacterized by deficient ossification of the parietal bones.Mutations in this gene also cause a form of frontonasal dysplasiawith alopecia and hypogonadism; suggesting a role for this gene incraniofacial development, mesenchymal-epithelial communication, andhair follicle development. Deletion of a segment of chromosome 11containing this gene, del(11)(p11p12), causes Potocki-Shaffersyndrome (PSS); a syndrome characterized by craniofacial anomalies,mental retardation, multiple exostoses, and genital abnormalitiesin males. In mouse, this gene has been shown to use dualtranslation initiation sites located 16 codons apart. [provided byRefSeq].
Other Names:
Homeobox protein aristaless-like 4, ALX4, KIAA1788
Gene Name: ALX4
Gene ID: 60529
Primary Accession: Q9H161
Other Accession: NP_068745.2
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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